JPH11269269A - アミノ官能性ポリオルガノシロキサン、その製法及びその使用 - Google Patents

アミノ官能性ポリオルガノシロキサン、その製法及びその使用

Info

Publication number: JPH11269269A
Authority: JP; Japan
Prior art keywords: group; amino; compound; functional polyorganosiloxane; general formula
Prior art date: 1998-01-21
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Pending

Application number

JP11009287A

Other languages

English (en)

Japanese (ja)

Inventor

Michael Messner

メースナーミヒャエル

Holger Rautschek

ラウチェクホルガー

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Huels AG

Original Assignee

Huels AG

Chemische Werke Huels AG

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1998-01-21

Filing date

1999-01-18

Publication date

1999-10-05

1999-01-18 Application filed by Huels AG, Chemische Werke Huels AG filed Critical Huels AG

1999-10-05 Publication of JPH11269269A publication Critical patent/JPH11269269A/ja

Status Pending legal-status Critical Current

Links

238000004519 manufacturing process Methods 0.000 title claims description 8
-1 mercaptosiloxane Chemical class 0.000 claims abstract description 39
125000000217 alkyl group Chemical group 0.000 claims abstract description 15
239000003999 initiator Substances 0.000 claims abstract description 12
125000002947 alkylene group Chemical group 0.000 claims abstract description 10
125000003396 thiol group Chemical class [H]S* 0.000 claims abstract description 8
125000003277 amino group Chemical group 0.000 claims abstract description 7
150000001875 compounds Chemical class 0.000 claims description 45
239000004753 textile Substances 0.000 claims description 22
125000004432 carbon atom Chemical group C* 0.000 claims description 18
238000006243 chemical reaction Methods 0.000 claims description 16
238000000034 method Methods 0.000 claims description 14
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims description 13
239000001257 hydrogen Substances 0.000 claims description 12
229910052739 hydrogen Inorganic materials 0.000 claims description 12
125000003118 aryl group Chemical group 0.000 claims description 8
238000002360 preparation method Methods 0.000 claims description 8
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 6
125000002877 alkyl aryl group Chemical group 0.000 claims description 6
239000007864 aqueous solution Substances 0.000 claims description 5
ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 claims description 5
125000005842 heteroatom Chemical group 0.000 claims description 5
150000002431 hydrogen Chemical class 0.000 claims description 5
239000004094 surface-active agent Substances 0.000 claims description 5
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 4
125000003545 alkoxy group Chemical group 0.000 claims description 4
125000005250 alkyl acrylate group Chemical group 0.000 claims description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 4
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 3
244000028419 Styrax benzoin Species 0.000 claims description 3
235000000126 Styrax benzoin Nutrition 0.000 claims description 3
235000008411 Sumatra benzointree Nutrition 0.000 claims description 3
229960002130 benzoin Drugs 0.000 claims description 3
235000019382 gum benzoic Nutrition 0.000 claims description 3
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 2
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 claims description 2
229920000536 2-Acrylamido-2-methylpropane sulfonic acid Polymers 0.000 claims description 2
XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 claims description 2
FKOZPUORKCHONH-UHFFFAOYSA-N 2-methylpropane-1-sulfonic acid Chemical group CC(C)CS(O)(=O)=O FKOZPUORKCHONH-UHFFFAOYSA-N 0.000 claims description 2
125000004810 2-methylpropylene group Chemical group [H]C([H])([H])C([H])(C([H])([H])[*:2])C([H])([H])[*:1] 0.000 claims description 2
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N Formic acid Chemical group OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 2
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical group NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 2
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 2
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 2
150000005215 alkyl ethers Chemical class 0.000 claims description 2
150000003868 ammonium compounds Chemical class 0.000 claims description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
239000000460 chlorine Substances 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 claims description 2
125000001033 ether group Chemical group 0.000 claims description 2
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 claims description 2
239000001530 fumaric acid Substances 0.000 claims description 2
125000003827 glycol group Chemical group 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 2
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
239000011976 maleic acid Substances 0.000 claims description 2
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 2
DYUWTXWIYMHBQS-UHFFFAOYSA-N n-prop-2-enylprop-2-en-1-amine Chemical compound C=CCNCC=C DYUWTXWIYMHBQS-UHFFFAOYSA-N 0.000 claims description 2
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 2
150000002978 peroxides Chemical class 0.000 claims description 2
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
229920006395 saturated elastomer Polymers 0.000 claims description 2
125000000565 sulfonamide group Chemical group 0.000 claims description 2
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims description 2
125000000101 thioether group Chemical group 0.000 claims description 2
125000004417 unsaturated alkyl group Chemical group 0.000 claims description 2
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims 1
150000008064 anhydrides Chemical class 0.000 claims 1
229910052799 carbon Inorganic materials 0.000 claims 1
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
239000000178 monomer Substances 0.000 abstract description 9
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 24
239000000047 product Substances 0.000 description 15
239000011248 coating agent Substances 0.000 description 14
238000000576 coating method Methods 0.000 description 14
239000000839 emulsion Substances 0.000 description 14
239000000203 mixture Substances 0.000 description 13
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
238000003756 stirring Methods 0.000 description 11
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 10
239000002904 solvent Substances 0.000 description 9
239000004744 fabric Substances 0.000 description 8
239000012299 nitrogen atmosphere Substances 0.000 description 8
229920001296 polysiloxane Polymers 0.000 description 7
239000000463 material Substances 0.000 description 6
238000005259 measurement Methods 0.000 description 6
239000000243 solution Substances 0.000 description 6
229920000742 Cotton Polymers 0.000 description 5
235000013870 dimethyl polysiloxane Nutrition 0.000 description 5
229910052757 nitrogen Inorganic materials 0.000 description 5
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 5
239000004205 dimethyl polysiloxane Substances 0.000 description 4
238000011156 evaluation Methods 0.000 description 4
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
238000010526 radical polymerization reaction Methods 0.000 description 4
238000010992 reflux Methods 0.000 description 4
239000000758 substrate Substances 0.000 description 4
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
238000005299 abrasion Methods 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
238000004945 emulsification Methods 0.000 description 3
150000002924 oxiranes Chemical group 0.000 description 3
239000000126 substance Substances 0.000 description 3
238000003786 synthesis reaction Methods 0.000 description 3
238000012360 testing method Methods 0.000 description 3
125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
LOOUJXUUGIUEBC-UHFFFAOYSA-N 3-(dimethoxymethylsilyl)propane-1-thiol Chemical compound COC(OC)[SiH2]CCCS LOOUJXUUGIUEBC-UHFFFAOYSA-N 0.000 description 2
UFQHFMGRRVQFNA-UHFFFAOYSA-N 3-(dimethylamino)propyl prop-2-enoate Chemical compound CN(C)CCCOC(=O)C=C UFQHFMGRRVQFNA-UHFFFAOYSA-N 0.000 description 2
YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
229910003849 O-Si Inorganic materials 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
229910003872 O—Si Inorganic materials 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
YTEISYFNYGDBRV-UHFFFAOYSA-N [(dimethyl-$l^{3}-silanyl)oxy-dimethylsilyl]oxy-dimethylsilicon Chemical compound C[Si](C)O[Si](C)(C)O[Si](C)C YTEISYFNYGDBRV-UHFFFAOYSA-N 0.000 description 2
NRTJGTSOTDBPDE-UHFFFAOYSA-N [dimethyl(methylsilyloxy)silyl]oxy-dimethyl-trimethylsilyloxysilane Chemical compound C[SiH2]O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C NRTJGTSOTDBPDE-UHFFFAOYSA-N 0.000 description 2
239000003513 alkali Substances 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
239000013011 aqueous formulation Substances 0.000 description 2
235000019400 benzoyl peroxide Nutrition 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
238000004821 distillation Methods 0.000 description 2
239000000835 fiber Substances 0.000 description 2
125000000524 functional group Chemical group 0.000 description 2
239000007789 gas Substances 0.000 description 2
IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical class CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 2
210000002741 palatine tonsil Anatomy 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
238000001556 precipitation Methods 0.000 description 2
WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
230000035484 reaction time Effects 0.000 description 2
239000005871 repellent Substances 0.000 description 2
239000007858 starting material Substances 0.000 description 2
238000009988 textile finishing Methods 0.000 description 2
239000008096 xylene Substances 0.000 description 2
238000004383 yellowing Methods 0.000 description 2
NFDXQGNDWIPXQL-UHFFFAOYSA-N 1-cyclooctyldiazocane Chemical compound C1CCCCCCC1N1NCCCCCC1 NFDXQGNDWIPXQL-UHFFFAOYSA-N 0.000 description 1
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
IUVCFHHAEHNCFT-INIZCTEOSA-N 2-[(1s)-1-[4-amino-3-(3-fluoro-4-propan-2-yloxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]ethyl]-6-fluoro-3-(3-fluorophenyl)chromen-4-one Chemical compound C1=C(F)C(OC(C)C)=CC=C1C(C1=C(N)N=CN=C11)=NN1[C@@H](C)C1=C(C=2C=C(F)C=CC=2)C(=O)C2=CC(F)=CC=C2O1 IUVCFHHAEHNCFT-INIZCTEOSA-N 0.000 description 1
TXFPEBPIARQUIG-UHFFFAOYSA-N 4'-hydroxyacetophenone Chemical compound CC(=O)C1=CC=C(O)C=C1 TXFPEBPIARQUIG-UHFFFAOYSA-N 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
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239000004952 Polyamide Substances 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
239000004902 Softening Agent Substances 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000003926 acrylamides Chemical class 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
230000002411 adverse Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
238000007098 aminolysis reaction Methods 0.000 description 1
150000001491 aromatic compounds Chemical class 0.000 description 1
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
239000012965 benzophenone Substances 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
230000033228 biological regulation Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
229930188620 butyrolactone Natural products 0.000 description 1
238000001460 carbon-13 nuclear magnetic resonance spectrum Methods 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
239000003431 cross linking reagent Substances 0.000 description 1
239000008367 deionised water Substances 0.000 description 1
229910021641 deionized water Inorganic materials 0.000 description 1
230000008021 deposition Effects 0.000 description 1
239000012973 diazabicyclooctane Substances 0.000 description 1
238000002845 discoloration Methods 0.000 description 1
238000004043 dyeing Methods 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
238000011067 equilibration Methods 0.000 description 1
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150000002148 esters Chemical class 0.000 description 1
230000005281 excited state Effects 0.000 description 1
238000001914 filtration Methods 0.000 description 1
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238000009472 formulation Methods 0.000 description 1
238000007429 general method Methods 0.000 description 1
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238000010559 graft polymerization reaction Methods 0.000 description 1
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238000006459 hydrosilylation reaction Methods 0.000 description 1
238000007654 immersion Methods 0.000 description 1
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239000010410 layer Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000011068 loading method Methods 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
238000000691 measurement method Methods 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
MKIJJIMOAABWGF-UHFFFAOYSA-N methyl 2-sulfanylacetate Chemical compound COC(=O)CS MKIJJIMOAABWGF-UHFFFAOYSA-N 0.000 description 1
239000004530 micro-emulsion Substances 0.000 description 1
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239000003960 organic solvent Substances 0.000 description 1
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239000005056 polyisocyanate Substances 0.000 description 1
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239000002244 precipitate Substances 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
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125000001302 tertiary amino group Chemical group 0.000 description 1
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229920002554 vinyl polymer Polymers 0.000 description 1
238000005406 washing Methods 0.000 description 1
230000037303 wrinkles Effects 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/38—Polysiloxanes modified by chemical after-treatment
- C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
- C08G77/392—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing sulfur
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C08G77/26—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen nitrogen-containing groups
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/12—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polysiloxanes
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/38—Polysiloxanes modified by chemical after-treatment
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/38—Polysiloxanes modified by chemical after-treatment
- C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
- C08G77/388—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing nitrogen
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
- D06M15/6433—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing carboxylic groups
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
- D06M15/6436—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing amino groups

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Textile Engineering (AREA)
Silicon Polymers (AREA)
Compositions Of Macromolecular Compounds (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Graft Or Block Polymers (AREA)

JP11009287A 1998-01-21 1999-01-18 アミノ官能性ポリオルガノシロキサン、その製法及びその使用 Pending JPH11269269A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE19802069.4		1998-01-21
DE19802069A DE19802069A1 (de)	1998-01-21	1998-01-21	Aminofunktionelle Polyorganosiloxane, deren Herstellung und Verwendung

Publications (1)

Publication Number	Publication Date
JPH11269269A true JPH11269269A (ja)	1999-10-05

Family

ID=7855195

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP11009287A Pending JPH11269269A (ja)	1998-01-21	1999-01-18	アミノ官能性ポリオルガノシロキサン、その製法及びその使用

Country Status (8)

Country	Link
US (1)	US6201093B1 (fr)
EP (1)	EP0930342A3 (fr)
JP (1)	JPH11269269A (fr)
KR (1)	KR19990068009A (fr)
CN (1)	CN1229807A (fr)
CA (1)	CA2259708A1 (fr)
DE (1)	DE19802069A1 (fr)
TW (1)	TW460507B (fr)

Cited By (4)

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JP2004331977A (ja) *	2003-05-08	2004-11-25	Wacker Chemie Gmbh	ポリアルコキシ基を有する有機ケイ素化合物およびその製法
JP2010518190A (ja) *	2007-02-06	2010-05-27	チバホールディングインコーポレーテッド	ポリシロキサンブロックコポリマー類
WO2014087779A1 (fr) *	2012-12-03	2014-06-12	花王株式会社	Polymère greffé à base d'organopolysiloxane
WO2015170536A1 (fr) *	2014-05-07	2015-11-12	富士フイルム株式会社	Solution de dispersion de pigment, élément décoratif, matériau de transfert pour former un élément décoratif, substrat doté d'un élément décoratif, écran tactile, dispositif d'affichage d'informations, polymère de silicone de type greffé

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DE10036693A1 (de) *	2000-07-27	2002-02-14	Wacker Chemie Gmbh	Verfahren zur Imprägnierung von Garnen
DE10036694A1 (de) *	2000-07-27	2002-02-14	Wacker Chemie Gmbh	Verfahren zur Behandlung von organischen Fasern mit aminofunktionellen Organosiliciumverbindungen
EP1195416A3 (fr)	2000-10-05	2005-12-28	Degussa AG	Nanocapsules organosiliciés polymérisables
EP1195417B1 (fr)	2000-10-05	2009-10-14	Evonik Degussa GmbH	Nanocapsules organosiliciés
DE10056344A1 (de)	2000-11-14	2002-05-16	Degussa	n-Propylethoxysiloxane, Verfahren zu deren Herstellung und deren Verwendung
DE50210398D1 (de)	2001-03-30	2007-08-16	Degussa	Siliciumorganische Nano-Mikrohybridsysteme oder Mikrohybridsysteme enthaltende Zusammensetzung für kratz- und abriebfeste Beschichtungen
EP1249470A3 (fr)	2001-03-30	2005-12-28	Degussa AG	Composition fortement chargée en nano et/ou microcapsules hybrides à base de silice organique pâteuse pour des revêtements résistants aux rayures et à l'abrasion
US6616980B2 (en)	2001-04-24	2003-09-09	Crompton Corporation	Emulsion polymerized acrylated silicone copolymer for wrinkle reduction
FR2824841B1 (fr) *	2001-05-15	2003-06-27	Rhodia Chimie Sa	Utilisation, dans une composition pour le traitement des articles en fibres textiles, d'un polyorganosiloxane a fonctions(s) piperidinyle (s) comme agent anti-salissure ("soil release")
US6824650B2 (en)	2001-12-18	2004-11-30	Kimberly-Clark Worldwide, Inc.	Fibrous materials treated with a polyvinylamine polymer
US7214633B2 (en) *	2001-12-18	2007-05-08	Kimberly-Clark Worldwide, Inc.	Polyvinylamine treatments to improve dyeing of cellulosic materials
US6911114B2 (en) *	2002-10-01	2005-06-28	Kimberly-Clark Worldwide, Inc.	Tissue with semi-synthetic cationic polymer
DE10253152A1 (de) *	2002-11-14	2004-06-03	Rudolf Gmbh & Co. Kg Chemische Fabrik	Teilquaternierte, aminofunktionelle Organopolysiloxane und deren Verwendung in wässrigen Systemen
DE10301976A1 (de) *	2003-01-20	2004-07-29	Wacker Polymer Systems Gmbh & Co. Kg	Silikonhaltige Polymerisate
DE102004025767A1 (de) *	2004-05-26	2005-12-22	Degussa Ag	Stabile Lösungen von N-substituierten Aminopolysiloxanen, deren Herstellung und Verwendung
FR2894993A1 (fr) *	2005-12-19	2007-06-22	Rhodia Recherches & Tech	Nouveau procede d'impregnation d'une surface textile
JP5000260B2 (ja) *	2006-10-19	2012-08-15	ＡｚエレクトロニックマテリアルズＩｐ株式会社	微細化されたパターンの形成方法およびそれに用いるレジスト基板処理液
ES2725499T3 (es)	2007-04-20	2019-09-24	Evonik Degussa Gmbh	Mezcla que contiene un compuesto de organosilicio y su uso
RU2010147447A (ru) *	2008-04-23	2012-05-27	Басф Се (De)	Доставка гидрофобных полезных агентов из моющих средств для тела и подобных в ороговевший субстрат
DE102008041920A1 (de)	2008-09-09	2010-03-11	Evonik Degussa Gmbh	Neue Katalysatoren für die Vernetzung von funktionellen Silanen oder funktionellen Siloxanen, insbesondere mit Substraten
JP5306755B2 (ja) *	2008-09-16	2013-10-02	ＡｚエレクトロニックマテリアルズＩｐ株式会社	基板処理液およびそれを用いたレジスト基板処理方法
CN101845144B (zh) *	2009-12-16	2013-01-30	上海诺科生物科技有限公司	水基型有机硅氟树脂防水剂及其制备方法
CN101851335B (zh) *	2010-05-26	2012-03-21	鲁东大学	双功能基修饰的硅胶吸附材料的制备方法及其在金属离子吸附中的应用
CN101914207B (zh) *	2010-09-04	2011-12-07	齐齐哈尔大学	一种亚麻柔软剂的合成方法
CN102153759B (zh) *	2011-03-16	2012-06-27	齐齐哈尔大学	两性聚硅氧烷亚麻柔软剂的合成方法
CN102505495B (zh) *	2011-11-10	2014-01-01	浙江传化股份有限公司	一种高弹平滑有机硅柔软剂及其制备方法和应用
CN105622944B (zh) *	2016-03-30	2018-08-07	科凯精细化工（上海）有限公司	一种季铵化有机硅油及其制备方法
CN105622945B (zh) *	2016-03-30	2018-09-14	科凯精细化工（上海）有限公司	一种增深整理剂及其制备方法
CN109400882B (zh) *	2018-10-29	2019-11-12	广州市斯洛柯高分子聚合物有限公司	一种氨羟基硅氧烷聚合物及其制备方法
CN109731557A (zh) *	2019-01-18	2019-05-10	贵州大学	含巯基修饰的微纳多级有机硅材料及其制备方法

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US3402191A (en)	1963-08-27	1968-09-17	Union Carbide Corp	N, n-disubstituted aminoalkylsiloxane copolymers and amine oxide, quaternary ammonium salt, and coordination compounds of transition metal derivatives thereof
US4071577A (en)	1976-04-23	1978-01-31	Dow Corning Corporation	Toughened mercaptosiloxane modified emulsion polymerized vinylic polymers
GB1570983A (en)	1976-06-26	1980-07-09	Dow Corning Ltd	Process for treating fibres
JPH01239175A (ja) *	1988-03-17	1989-09-25	Nisshin Kagaku Kogyo Kk	繊維処理剤
EP0342830B1 (fr)	1988-05-17	1995-01-11	Dow Corning Limited	Composés organosiliciques
GB9002715D0 (en)	1990-02-07	1990-04-04	Dow Corning	Method of treating fibrous materials
JPH04119174A (ja) *	1990-09-10	1992-04-20	Toray Dow Corning Silicone Co Ltd	繊維処理剤
US5468477A (en) *	1992-05-12	1995-11-21	Minnesota Mining And Manufacturing Company	Vinyl-silicone polymers in cosmetics and personal care products
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FR2714402B1 (fr) *	1993-12-27	1996-02-02	Rhone Poulenc Chimie	Procédé d'adoucissage textile non jaunissant dans lequel on utilise une composition comprenant un polyorganosiloxane.
DE4424914A1 (de)	1994-07-14	1996-01-18	Wacker Chemie Gmbh	Aminofunktionelle Organopolysiloxane

1998
- 1998-01-21 DE DE19802069A patent/DE19802069A1/de not_active Withdrawn
1999
- 1999-01-08 EP EP99100229A patent/EP0930342A3/fr not_active Withdrawn
- 1999-01-18 JP JP11009287A patent/JPH11269269A/ja active Pending
- 1999-01-20 US US09/233,201 patent/US6201093B1/en not_active Expired - Fee Related
- 1999-01-20 TW TW088100817A patent/TW460507B/zh not_active IP Right Cessation
- 1999-01-20 KR KR1019990001572A patent/KR19990068009A/ko not_active Withdrawn
- 1999-01-20 CA CA002259708A patent/CA2259708A1/fr not_active Abandoned
- 1999-01-20 CN CN99101330A patent/CN1229807A/zh active Pending

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2004331977A (ja) *	2003-05-08	2004-11-25	Wacker Chemie Gmbh	ポリアルコキシ基を有する有機ケイ素化合物およびその製法
JP2010518190A (ja) *	2007-02-06	2010-05-27	チバホールディングインコーポレーテッド	ポリシロキサンブロックコポリマー類
WO2014087779A1 (fr) *	2012-12-03	2014-06-12	花王株式会社	Polymère greffé à base d'organopolysiloxane
JP2014109004A (ja) *	2012-12-03	2014-06-12	Kao Corp	オルガノポリシロキサングラフトポリマー
CN104812790A (zh) *	2012-12-03	2015-07-29	花王株式会社	有机聚硅氧烷接枝聚合物
US9351920B2 (en)	2012-12-03	2016-05-31	Kao Corporation	Organopolysiloxane graft polymer
WO2015170536A1 (fr) *	2014-05-07	2015-11-12	富士フイルム株式会社	Solution de dispersion de pigment, élément décoratif, matériau de transfert pour former un élément décoratif, substrat doté d'un élément décoratif, écran tactile, dispositif d'affichage d'informations, polymère de silicone de type greffé
CN106232735A (zh) *	2014-05-07	2016-12-14	富士胶片株式会社	颜料分散液、装饰材、装饰材形成用的转印材料、带装饰材的基材、触摸屏、信息显示装置、接枝型硅酮聚合物
CN106232735B (zh) *	2014-05-07	2019-07-19	富士胶片株式会社	颜料分散液与其用途、以及接枝型硅酮聚合物

Also Published As

Publication number	Publication date
CN1229807A (zh)	1999-09-29
EP0930342A3 (fr)	2000-10-11
CA2259708A1 (fr)	1999-07-21
DE19802069A1 (de)	1999-07-22
EP0930342A2 (fr)	1999-07-21
US6201093B1 (en)	2001-03-13
TW460507B (en)	2001-10-21
KR19990068009A (ko)	1999-08-25

Publication	Publication Date	Title
JPH11269269A (ja)	1999-10-05	アミノ官能性ポリオルガノシロキサン、その製法及びその使用
US5196260A (en)	1993-03-23	Process for the treatment of fibrous materials with modified organopolysiloxanes and the materials
US7153922B2 (en)	2006-12-26	Organosilicon compounds having polyoxyalkylene radicals
JP2821494B2 (ja)	1998-11-05	ポリジオルガノシロキサン、その製法及びそれを含有する繊維被覆剤
KR100524038B1 (ko)	2006-01-27	힌더드4-아미노-3,3-디메틸부틸기를갖는신규한아미노폴리실록산
CN105601799B (zh)	2018-03-16	核/壳型有机硅改性丙烯酸酯乳液及其制备方法和应用
US7855264B2 (en)	2010-12-21	Polymeric products useful as oil repellents
JPS61123635A (ja)	1986-06-11	オキシアルキレン単位がグラフト結合されたポリオルガノシロキサン及びその製法
JP2001115030A (ja)	2001-04-24	アミン、ポリオール、官能性シロキサン類を含む繊維処理組成物
JPH01239175A (ja)	1989-09-25	繊維処理剤
JPH069876A (ja)	1994-01-18	架橋結合可能な組成物、オルガノポリシロキサン化合物、その製法、そのエマルジョン又はマイクロエマルジョンの製法及び有機繊維及び織物の処理法
JP2513979B2 (ja)	1996-07-10	アシル化されたアミノ官能性オルガノポリシロキサンを含有する乳濁液の製造法
CN102164976A (zh)	2011-08-24	氟硅氧烷和表面处理剂
KR940008993B1 (ko)	1994-09-28	자기가교성 아미노실록산 에멀젼의 제조방법
KR100798186B1 (ko)	2008-01-24	발수성 텍스타일 마무리제 및 제조방법
JPH02175973A (ja)	1990-07-09	繊維状材料を変性されたオルガノポリシロキサンで処理する方法及びこの様に処理された材料
EP1735359B1 (fr)	2008-09-24	Produits de reaction polymeres issus d'aminosiloxanes substitues
JPH10140480A (ja)	1998-05-26	繊維処理剤
CN110267998A (zh)	2019-09-20	用于疏水性和疏油性织物整理的聚合物
EP1282656B1 (fr)	2004-02-11	Melanges de polyorganosiloxanes destines au traitement des matieres fibreuses
JPS584114B2 (ja)	1983-01-25	羊毛を防縮加工するための調製剤
JP2000129579A (ja)	2000-05-09	モノアクリレ―トポリエ―テルで処理した繊維
JP2648515B2 (ja)	1997-09-03	セルロース系繊維の処理方法
JPH11158287A (ja)	1999-06-15	ジオルガノポリシロキサンおよび固体処理剤
JPH0995535A (ja)	1997-04-08	ジオルガノポリシロキサンおよび布帛用処理剤